FDA 510(k)

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube

K-Number: K230493 · 2023-11-27

Decision Date2023-11-27

Product CodeGIM

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2023-11-27 under 510(k) number K230493. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube?

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube is a medical device that received FDA 510(k) clearance on 2023-11-27. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K230493.

When did BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube receive FDA 510(k) clearance?

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube received FDA 510(k) clearance on 2023-11-27, under 510(k) number K230493.

Who is the listed applicant for BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube?

The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube?

The FDA product code for BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube is GIM.

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Other records listing Becton, Dickinson and Company as applicant

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Related Devices (Code: GIM)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.